A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332186



Internal ID20865355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185578386..185579552hg38UCSC Ensembl
chr1:185547518..185548684hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381167
hg191167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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